Canonical Allele Identifier: CA2207531707

Linked Data

dbSNP Id: rs2069950297

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.11281331G>A , CM000678.2:g.11281331G>A GRCh38
NC_000016.9:g.11375188G>A , CM000678.1:g.11375188G>A GRCh37
NC_000016.8:g.11282689G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000649869.1:n.152+31553G>A (RMI2)
ENST00000312511.3:c.-93C>T (PRM1) ENSP00000310515.3:n.-93C>T
ENST00000572173.1:c.-515-13885G>A (RMI2) ENSP00000461206.1:n.-515-13885G>A
ENST00000573910.1:n.160+31553G>A (RMI2)
NM_002761.2:c.-93C>T (PRM1) NP_002752.1:n.-93C>T
XR_933070.1:n.733+31553G>A
XR_933070.3:n.876+31553G>A